Considering the Genetic Architecture of Hypoplastic Left Heart Syndrome

por Belmont, John W.
Publicado 2022

Estimating the burden and economic impact of pediatric genetic disease

por Gonzaludo, Nina, Belmont, John W., Gainullin, Vladimir G., Taft, Ryan J.
Publicado 2018

Correction: Estimating the burden and economic impact of pediatric genetic disease

por Gonzaludo, Nina, Belmont, John W., Gainullin, Vladimir G., Taft, Ryan J.
Publicado 2019

SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencing

por Tariq, Muhammad, Belmont, John W, Lalani, Seema, Smolarek, Teresa, Ware, Stephanie M
Publicado 2011

Analysis of East Asia Genetic Substructure Using Genome-Wide SNP Arrays

por Tian, Chao, Kosoy, Roman, Lee, Annette, Ransom, Michael, Belmont, John W., Gregersen, Peter K., Seldin, Michael F.
Publicado 2008

Assessing the utility of whole-genome amplified serum DNA for array-based high throughput genotyping

por Bucasas, Kristine L, Pandya, Gagan A, Pradhan, Sonal, Fleischmann, Robert D, Peterson, Scott N, Belmont, John W
Publicado 2009

The diagnostic trajectory of infants and children with clinical features of genetic disease

por Schroeder, Brock E., Gonzaludo, Nina, Everson, Katie, Than, Kyi-Sin, Sullivan, Jeff, Taft, Ryan J., Belmont, John W.
Publicado 2021

European Population Substructure: Clustering of Northern and Southern Populations

por Seldin, Michael F, Shigeta, Russell, Villoslada, Pablo, Selmi, Carlo, Tuomilehto, Jaakko, Silva, Gabriel, Belmont, John W, Klareskog, Lars, Gregersen, Peter K
Publicado 2006

Congenital sucrase-isomaltase deficiency presenting with failure to thrive, hypercalcemia, and nephrocalcinosis

por Belmont, John W, Reid, Barbara, Taylor, William, Baker, Susan S, Moore, Warren H, Morriss, Michael C, Podrebarac, Susan M, Glass, Nancy, Schwartz, I David
Publicado 2002

Prior Infections With Seasonal Influenza A/H1N1 Virus Reduced the Illness Severity and Epidemic Intensity of Pandemic H1N1 Influenza in Healthy Adults

por Couch, Robert B., Atmar, Robert L., Franco, Luis M., Quarles, John M., Niño, Diane, Wells, Janet M., Arden, Nancy, Cheung, Sheree, Belmont, John W.
Publicado 2012

The Medical Genome Initiative: moving whole-genome sequencing for rare disease diagnosis to the clinic

por Marshall, Christian R., Bick, David, Belmont, John W., Taylor, Stacie L., Ashley, Euan, Dimmock, David, Jobanputra, Vaidehi, Kearney, Hutton M., Kulkarni, Shashikant, Rehm, Heidi
Publicado 2020

Replicative mechanisms for CNV formation are error prone

por Carvalho, Claudia M. B., Pehlivan, Davut, Ramocki, Melissa B., Fang, Ping, Alleva, Benjamin, Franco, Luis M., Belmont, John W., Hastings, P. J., Lupski, James R.
Publicado 2013

SNP genotyping to screen for a common deletion in CHARGE Syndrome

por Lalani, Seema R, Safiullah, Arsalan M, Fernbach, Susan D, Phillips, Michael, Bacino, Carlos A, Molinari, Laura M, Glass, Nancy L, Towbin, Jeffrey A, Craigen, William J, Belmont, John W
Publicado 2005

Clinical utility of genomic sequencing: a measurement toolkit

por Hayeems, Robin Z., Dimmock, David, Bick, David, Belmont, John W., Green, Robert C., Lanpher, Brendan, Jobanputra, Vaidehi, Mendoza, Roberto, Kulkarni, Shashi, Grove, Megan E., Taylor, Stacie L., Ashley, Euan
Publicado 2020

Low Levels of Genetic Divergence across Geographically and Linguistically Diverse Populations from India

por Rosenberg, Noah A, Mahajan, Saurabh, Gonzalez-Quevedo, Catalina, Blum, Michael G. B, Nino-Rosales, Laura, Ninis, Vasiliki, Das, Parimal, Hegde, Madhuri, Molinari, Laura, Zapata, Gladys, Weber, James L, Belmont, John W, Patel, Pragna I
Publicado 2006

An ancestry informative marker set for determining continental origin: validation and extension using human genome diversity panels

por Nassir, Rami, Kosoy, Roman, Tian, Chao, White, Phoebe A, Butler, Lesley M, Silva, Gabriel, Kittles, Rick, Alarcon-Riquelme, Marta E, Gregersen, Peter K, Belmont, John W, De La Vega, Francisco M, Seldin, Michael F
Publicado 2009

Host Transcriptional Response to Influenza and Other Acute Respiratory Viral Infections – A Prospective Cohort Study

por Zhai, Yijie, Franco, Luis M., Atmar, Robert L., Quarles, John M., Arden, Nancy, Bucasas, Kristine L., Wells, Janet M., Niño, Diane, Wang, Xueqing, Zapata, Gladys E., Shaw, Chad A., Belmont, John W., Couch, Robert B.
Publicado 2015

Integrative genomic analysis of the human immune response to influenza vaccination

por Franco, Luis M, Bucasas, Kristine L, Wells, Janet M, Niño, Diane, Wang, Xueqing, Zapata, Gladys E, Arden, Nancy, Renwick, Alexander, Yu, Peng, Quarles, John M, Bray, Molly S, Couch, Robert B, Belmont, John W, Shaw, Chad A
Publicado 2013

Correction: Integrative genomic analysis of the human immune response to influenza vaccination

por Franco, Luis M, Bucasas, Kristine L, Wells, Janet M, Niño, Diane, Wang, Xueqing, Zapata, Gladys E, Arden, Nancy, Renwick, Alexander, Yu, Peng, Quarles, John M, Bray, Molly S, Couch, Robert B, Belmont, John W, Shaw, Chad A
Publicado 2016

Postmortem genetic screening for the identification, verification, and reporting of genetic variants contributing to the sudden death of the young

por Methner, D. Nicole R., Scherer, Steven E., Welch, Katherine, Walkiewicz, Magdalena, Eng, Christine M., Belmont, John W., Powell, Mark C., Korchina, Viktoriya, Doddapaneni, Harsha Vardhan, Muzny, Donna M., Gibbs, Richard A., Wolf, Dwayne A., Sanchez, Luis A., Kahn, Roger
Publicado 2016